Configure to the protocol, then size to the patient group:
| Component | Typical specification | Options |
|---|---|---|
| Endotracheal tube | Cuffed / uncuffed, sized to group | Adult, paediatric, neonatal size range |
| Airway adjuncts | Oropharyngeal / nasopharyngeal | Size range per pack |
| Suction catheter | Sterile, sized to tube | Included or supplied separately |
| Syringe for cuff | Luer, sized to cuff pilot | Standard inclusion |
| Lubricant | Sterile, water-soluble | Included or supplied separately |
| Securing device | Tie or holder | Type per unit protocol |
| Gloves and drape | Sterile field items | Size and format per protocol |
Note: contents are configured to the airway protocol of the ordering department and versioned thereafter.
Airway consumables are assessed on reliability under time pressure:
Yes. We work from the contents your team actually uses for a standard intubation in your department, including items such as the securing device that generic packs often omit. The configuration is agreed with your clinical team, then versioned so subsequent production runs are identical and changes require your approval.
For most departments, yes. Tube size range, adjunct sizes and even suction catheter sizing differ enough between groups that a single kit carries items wrong for both. Two configurations, one adult and one paediatric or neonatal, cover the caseload better than one universal pack — and the paediatric kit is used often enough to justify stocking it rather than assembling it.
It can be included or supplied separately, depending on how your department works — some units keep suction on the machine rather than in the pack. Confirm at configuration stage, since this changes both the contents and the pack dimensions. Including them removes a step during the procedure at the cost of a slightly larger pack.
Cuff inflation, leak-tightness and pilot balloon and valve function are checked at batch level, and tube dimensions are verified against specification. A cuff failure during a case means the airway has to be re-established immediately, so this is treated as a critical characteristic rather than a routine check.
Shelf life is stated on the label and supported by validated packaging and accelerated aging data under ISO 11607. Storage is at ambient temperature, dry, out of direct sunlight, with the pouch unopened until use. Expiry and lot are printed on both the unit pack and the outer carton so stock rotation works on a shelf.
Yes. Kits are produced with your brand, artwork, part numbers and IFU, including the label content your market requires — lot, expiry, sterilization method, legal manufacturer and, where applicable, the EU Authorised Representative. Artwork and label verification are part of the project.
Parent and related categories:
Anesthesia Consumables ·
Anesthesia Puncture Kit ·
Interventional Consumables
OEM & manufacturing:
Custom Procedure Packs ·
OEM Infusion & Nursing Consumables ·
Factory Audit & Visit
Regulatory guides for your market:
EU MDR Import Requirements ·
UAE MOHAP Registration ·
All Regulatory Guides
Who we supply:
Hospital Procurement ·
Become a Distributor
Technical reading:
Pack Design and OR Efficiency ·
Developing Custom Procedure Packs ·
ISO 11607 Packaging Validation
Need a Disposable Endotracheal Intubation Kit matched to your airway protocol?
Send us the contents list your team uses for a standard intubation, plus your patient groups. We will propose a configured pack, sequenced in the order the procedure runs, with a per-kit price.
A sample pack can be built for clinical review before you commit.